To understand the normalization process in families with hemophiliac children, and to explore the impact of two different therapeutic regimes on it (on-demand therapy and prophylaxis), we conducted a two-phase study using semistructured interviews. In the course of the first phase, we interviewed 13 parents belonging to 10 families with hemophiliac children in on-demand therapy. In the second phase, 5 years later, we repeated the interviews with three families who began prophylaxis at different times. We analyzed the interviews using text analysis software. The results show very different representations of hemophilia and daily life. Normalization processes involve the overcoming of a divided conception of life, and encourage the integration of care practices within daily life. Moreover, in our article we suggest that although prophylaxis facilitates the recovery of a regular family routine, it alone cannot produce normalization.

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http://dx.doi.org/10.1177/1049732311417456DOI Listing

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Article Synopsis
  • Reliable health-related quality of life data is essential for advocating national hemophilia care programs in developing countries, as demonstrated by this study focused on adolescents in Hubei Province.
  • The study involved 84 hemophilia patients aged 8 to 18 and used specific questionnaires to evaluate their quality of life, revealing an average score lower than that of peers in developed countries.
  • Key factors affecting their quality of life included residence, family income, and type of hemophilia, highlighting the need for improved healthcare access, psychological support, and targeted policy measures to enhance treatment conditions.
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Introduction And Importance: Haemophilia A (HA) is a hereditary X-linked recessive hemorrhagic disorder that results from a deficiency or dysfunction of coagulation factor VIII (FVIII) caused by gene mutations.

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